Standalone Multiple Sequence alignment tool
6
1
Entering edit mode
8.2 years ago
Eva_Maria ▴ 190

Can any one suggest a standalone Multiple Sequence alignment tool which gives alignment fasta as out put rather than MAFFT

alignment Assembly sequencing • 4.1k views
ADD COMMENT
0
Entering edit mode

Any particular reason you dislike MAFFT? In my experience it is one of the best tools out there in terms of the quality of alignments it produces

ADD REPLY
0
Entering edit mode

Agreed. We use MAFFT within our MSA editor (Base-By-Base)

ADD REPLY
1
Entering edit mode
8.2 years ago
EVR ▴ 610

jalview is best tool for MSA. Give a try, you will like it

ADD COMMENT
1
Entering edit mode
8.2 years ago
Charles Plessy ★ 2.9k

We have quite a lot of them packaged in Debian, plus the EMBOSS package that can convert multiple sequence alignment outputs from one format to the other.

ADD COMMENT
0
Entering edit mode
8.2 years ago
dago ★ 2.8k

I guess you have quite some options. I personally use muscle most of the time.

ADD COMMENT
0
Entering edit mode
7.8 years ago
Suzanne ▴ 100

Jalview is a free protein and nucleic acid sequence alignment visualisation software. It can be launch from http://www.jalview.org/. There are several Jalview 'how-to' videos on the Jalview YouTube training channel (https://www.youtube.com/channel/UCIjpnvZB770yz7ftbrJ0tfw). I recommend the one on 'Saving alignments, trees, 3D structures, annotations and projects in Jalview' at https://youtu.be/zXrOlOsyZdc.

ADD COMMENT
0
Entering edit mode
7.8 years ago
st.ph.n ★ 2.7k

Multiple Sequence Alignment Tools You should consider the length and number of sequences to see if the tool can handle it. Personally, I would use clustal, and parse the .aln file into a fasta.

ADD COMMENT
0
Entering edit mode
7.1 years ago
Cupton ▴ 80

Jalview is great, but focuses on proteins. Have a look at Base-By-Base: https://virology.uvic.ca/virology-ca-tools/base-by-base/

This can handle genes, proteins, viral genomes (up to 400 kb). It has a different set of modules than Jalview.

It makes editing MSAs easy and displays the differences between sequences so that it's easy to use.

It has the ability to find SNPs that are in seqs A, B and C, but not in seqs D or E. (and more complicated logic)

ADD COMMENT
0
Entering edit mode

Base-By-Base uses ClustalO, Muscle or MAFFT for alignments

ADD REPLY

Login before adding your answer.

Traffic: 1771 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6